Intercontinental dissemination of IMP-13-producing Pseudomonas aeruginosa belonging in sequence type 621.

IMP-type metallo-lactamases (MBLs) were the first acquired MBLs detected in Gram-negative pathogens, in the early 1990s, and are among the most relevant due to their worldwide distribution (12, 18). Several IMP-type variants have been described (3). IMP-13 was first detected in clinical isolates of Pseudomonas aeruginosa from Italy (16), where IMP-13 has become a widespread carbapenem resistance determinant, even involved in relatively large outbreaks (11, 13, 17). IMP-13 was also occasionally detected in P. aeruginosa isolates from other European countries, including Austria (7), Romania (9), and France (6). Interestingly, the IMP13-producing Italian isolates were found to belong in the same clonal lineage (13), and a clonal relationship with this lineage was also demonstrated for a Romanian isolate (9). In these isolates, the blaIMP-13 gene was found to be carried in different class 1 integron structures (InPSG, In88, and In89), usually located on the chromosome or, more rarely, on plasmids (11, 13, 16). IMP-13-producing P. aeruginosa isolates have also been detected in Argentina, where IMP-13 and IMP-16 represent the only IMP-type MBLs thus far reported (1, 4, 15). In this work, we investigated 20 IMP-13-producing P. aeruginosa isolates (19 clinical isolates and 1 environmental isolate) from an outbreak in Argentina (15) and compared them with P. aeruginosa AV65, as a representative of the IMP-13-producing clone spreading in Italy (13). The IMP-13-producing isolate from Romania (Pa247), previously described as clonally related to the Italian clone (9), was also included in the comparative analysis. Pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) were performed according to published protocols (5, 10). Sequence type (ST) numbers were assigned using the pubMLST database (http://pubmlst.org/paeruginosa/). Characterization of the variable region of class 1 integrons and their 5 flanking sequences were performed by a PCR mapping and sequencing approach as previously reported (11, 16). The chromosomal or plasmid location of the -lactamase gene was investigated by the I-CeuI and S1 nuclease-mapping techniques as described previously (2, 8). Under the assayed conditions, S1 digestion converts plasmids to linear DNA forms without cutting the genomic DNA (2), while I-CeuI only cuts into the genomic DNA (8). Following digestion with SpeI, all the Argentinean isolates exhibited PFGE profiles that were identical or different by no more than three bands (Fig. 1), revealing clonal relatedness. A total of 8 clonal variants (A1 to A8) were identified (Fig. 1). The PFGE profiles of the Argentinean isolates appeared to be also related with that of AV65, with a difference of 2 to 6 bands (Fig. 1), suggesting a possible clonal relatedness between the Argentinean isolates and the Italian epidemic clone. By MLST analysis, the AV65 and Pa247 isolates and all the Argentinean isolates were identified as belonging in ST621. Interestingly, the same ST was also reported for the IMP-13-producing isolate from Austria (7). Altogether, these results revealed a common genetic lineage for the IMP-13-producing P. aeruginosa isolates circulating worldwide. Characterization of the variable regions of the class 1 integrons carrying the blaIMP-13 cassette from the P. aeruginosa isolates from Argentina revealed structures identical to those previously found in European isolates. In particular, most Argentinean isolates harbored integron InPSG (11, 13), which was also the most common integron platform among Italian isolates (13) and that found in isolates from Romania (9) and Austria (7). Moreover, sequence analysis showed that InPSG from the Argentinean isolates was inserted into a Tn5051-like transposon at the same res insertion site already described for the InPSG-harboring Italian isolates (11), suggesting a common origin for these genetic structures. In the remaining Argentinean isolate, the blaIMP-13 cassette was carried as a single gene cassette by In88, which was also described to occur in one of the IMP-13-producing Italian isolates (13) and could be derived from InPSG by excision of the aacA4 cassette present in the second position. Efforts aimed at purifying plasmids carrying blaIMP-13 (14) or transferring the resistance determinant by conjugation (11) or transformation (14) were unsuccessful. Southern blot hybridization, using a blaIMP-13 probe and a 16S rRNA probe after I-CeuI digestion and PFGE separation, showed that the blaIMP gene was chromosomally located, since the bands that hybridized with the blaIMP probe also hybridized with the 16S rRNA probe. Southern blot analysis of PFGE of SpeI-restricted genomic DNAs with the blaIMP probe detected the resistance marker in the same fragment in all isolates, while for a single isolate the resistance marker was also detected in an additional fragment, suggesting the possibility of in vivo rearrangement events when the resistance determinant is carried on transposable genetic structures (data not shown). The overall genomic relatedness of the IMP-13-producing isolates and the fact that the blaIMP-13 gene was inserted in a conserved genetic context point to a common ancestry for the